Silversocks may go a very small way towards helping people suffering from Epidermolysis Bullosa (EB), but we appreciate that sufferers of this condition and their families need all the support they can get, so we will repeat this blog post every month to encourage visitors to our site to find out more about the condition and if possible support DEBRA in all the work they do.
DEBRA International is a worldwide network of national groups working on behalf of those affected by the genetic skin blistering condition Epidermolysis Bullosa.
If you are interested in supporting DEBRA International or EB patients nationally, you will find options to do so on their website: www.debra-international.org/debra.html
